- Optimising and revising SOPs, Batch Records and Work Instructions- Maintaining GMP compliance- Managing change controls and deviations- Documentation associated with manufacturing - Ensuring the cleanroom is in an optimised state- Improving processes
- MBO in life sciences- 2+ years cGMP work experience in a biotech or pharmaceutical manufacturing environment- Data analysis, Microsoft and Excel expertise - Flexible to work in shifts- Able to lift over 15kg- Fluent in English
Information available upon request.
Conditions of employment are up to market standard.
Uren per week: 36 - 40
Please send your application through our website.
Lisanne Keir +31 (0) 88 035 1994 firstname.lastname@example.org